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Interleukin-32 Gamma as a New Face in Inflammatory Bone Diseases

  • Lee, Eun-Jin (Department of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Choi, Bongkun (Department of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Hwang, Eui-Seung (Department of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Chang, Eun-Ju (Department of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine)
  • Received : 2017.02.13
  • Accepted : 2017.02.14
  • Published : 2017.02.28

Abstract

Interleukin-32 (IL-32), a recently identified pro-inflammatory cytokine, is involved in the pathogenesis and progression of infections, cancer, chronic inflammation, and autoimmune disease. IL-32γ is the most active isoform in cell death and cell activation among nine distinct isoforms of IL-32. IL-32γ potentiates both osteogenic and osteoclastogenic capacities, and is critical in the coupling of bone resorption and bone formation for maintenance of bone homeostasis. IL-32γ is strongly associated with inflammatory bone disorders such as rheumatoid arthritis, ankylosing spondylitis, and osteoporosis. In this review, we summarize current research on the role of IL-32γ in inflammatory bone disorders, highlighting this cytokine as a novel target for prognostic marker and control of these diseases.

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Acknowledgement

This work was supported by grants from the Basic Science Research Program funded by the Ministry of Education, Science, and Technology (2016R1DA1B039-33855 and NRF-2014R1A1A2056099).